Canonical Allele Identifier: CA2614624666

Gene: AIP

Linked Data

• gnomAD v4: 11-67490539-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490540_67490541del , CM000673.2:g.67490540_67490541del	GRCh38
NC_000011.9:g.67258011_67258012del , CM000673.1:g.67258011_67258012del	GRCh37
NC_000011.8:g.67014587_67014588del	NCBI36
NG_008969.1:g.12507_12508del , LRG_460:g.12507_12508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.847_848del
ENST00000528641.7:c.598+83_598+84del	ENSP00000434982.3:n.598+83_598+84del
ENST00000529797.2:n.1382_1383del
ENST00000682324.1:c.469-457_469-456del	ENSP00000508017.1:n.469-457_469-456del
ENST00000682659.1:c.418+83_418+84del	ENSP00000507351.1:n.418+83_418+84del
ENST00000682699.1:c.787+83_787+84del	ENSP00000507935.1:n.787+83_787+84del
ENST00000683237.1:c.779+91_779+92del	ENSP00000507343.1:n.779+91_779+92del
ENST00000683856.1:c.610+83_610+84del	ENSP00000507979.1:n.610+83_610+84del
ENST00000684006.1:c.787+83_787+84del	ENSP00000507269.1:n.787+83_787+84del
ENST00000684657.1:c.607+83_607+84del	ENSP00000507961.1:n.607+83_607+84del
ENST00000279146.8:c.787+83_787+84del MANE Select	ENSP00000279146.3:n.787+83_787+84del
ENST00000279146.7:c.787+83_787+84del	ENSP00000279146.3:n.787+83_787+84del
ENST00000525341.1:c.522_523del	ENSP00000476993.1:p.Ala175LeufsTer7
ENST00000528641.6:c.598+83_598+84del	ENSP00000434982.2:n.598+83_598+84del
NM_001302959.1:c.610+83_610+84del	NP_001289888.1:n.610+83_610+84del
NM_001302960.1:c.779+91_779+92del	NP_001289889.1:n.779+91_779+92del
NM_003977.3:c.787+83_787+84del	NP_003968.3:n.787+83_787+84del
XM_024448761.1:c.787+83_787+84del	XP_024304529.1:n.787+83_787+84del
NM_003977.4:c.787+83_787+84del MANE Select	NP_003968.3:n.787+83_787+84del
NM_001302960.2:c.779+91_779+92del	NP_001289889.1:n.779+91_779+92del
NM_001302959.2:c.610+83_610+84del	NP_001289888.1:n.610+83_610+84del